Job Description
Medical Information Manager
A leading pharmaceutical company is looking for an experienced Medical Information Manager to join their European Medical Affairs team.
This is a highly cross-functional role, supporting internal stakeholders and external service providers with accurate, timely, and scientifically balanced medical information across a portfolio of innovative products.
Key Responsibilities:
* Act as a therapy area expert, delivering second-line medical information support across European affiliates and commercial teams.
* Collaborate closely with external medical information providers, ensuring compliance and high-quality service delivery.
* Create, update, and manage scientific response documents.
* Respond to complex medical enquiries from healthcare professionals and patients.
* Conduct literature reviews and critically appraise data for inclusion in medical content.
* Support promotional material review (including job bag and copy approval).
* Provide training and ongoing support to contact center partners.
* Analyze enquiry trends and deliver actionable insights to internal stakeholders.
* Represent the company at medical congresses and staff Medical Information booths.
Requirements:
* Degree in Pharmacy (or equivalent scientific qualification).
* 4–6 years of Medical Information experience, ideally in a large pharma setting.
* Strong knowledge of EFPIA/ABPI Codes of Practice and PIPA guidelines.
* Proven expertise in medical writing and content development.
* Working knowledge of PromoMat and IRMS systems is desirable.
* Experience with medical review of promotional and non-promotional materials.
* Familiarity with Pharmacovigilance and compliance processes.
* Comfortable working in a European or regional role across multiple markets.
You will thrive in this role if you:
* Are highly detail-oriented with strong critical appraisal skills.
* Communicate clearly and collaborate well in cross-functional teams.
* Are proactive, adaptable, and customer-focused.
* Stay up to date with industry best practices and evolving regulations.
Why Join?
This is a chance to play a central role in supporting the scientific and medical integrity of a highly respected pharmaceutical portfolio.
You will work alongside passionate colleagues in Medical Affairs, Regulatory, Quality, and Commercial - contributing to the delivery of trusted information that matters.
Ready to take the next step?
Apply in confidence or get in touch to learn more.
We welcome applicants from diverse backgrounds and are committed to creating an inclusive workplace.